WO2019071153A1 - PROGRAMMABLE DENDRITIC MEDICINES - Google Patents
PROGRAMMABLE DENDRITIC MEDICINES Download PDFInfo
- Publication number
- WO2019071153A1 WO2019071153A1 PCT/US2018/054648 US2018054648W WO2019071153A1 WO 2019071153 A1 WO2019071153 A1 WO 2019071153A1 US 2018054648 W US2018054648 W US 2018054648W WO 2019071153 A1 WO2019071153 A1 WO 2019071153A1
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- WIPO (PCT)
- Prior art keywords
- compound
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- compounds
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- 0 CC(CO)NC(C(*)C(C=CC)=C)=C Chemical compound CC(CO)NC(C(*)C(C=CC)=C)=C 0.000 description 2
- CRURPZYEEOSWMH-UHFFFAOYSA-N CC(C)Cc1ccc(C(C)C(NC(CO)CO)=O)cc1 Chemical compound CC(C)Cc1ccc(C(C)C(NC(CO)CO)=O)cc1 CRURPZYEEOSWMH-UHFFFAOYSA-N 0.000 description 1
- GKBIYHJLCVDJAP-UHFFFAOYSA-N CC(C)Cc1ccc(C(C)C(ON(C(CC2)=O)C2=O)=O)cc1 Chemical compound CC(C)Cc1ccc(C(C)C(ON(C(CC2)=O)C2=O)=O)cc1 GKBIYHJLCVDJAP-UHFFFAOYSA-N 0.000 description 1
- QWTBDIBOOIAZEF-UHFFFAOYSA-N CC(C)N(C(C)C)P(OCCC#N)Cl Chemical compound CC(C)N(C(C)C)P(OCCC#N)Cl QWTBDIBOOIAZEF-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6889—Conjugates wherein the antibody being the modifying agent and wherein the linker, binder or spacer confers particular properties to the conjugates, e.g. peptidic enzyme-labile linkers or acid-labile linkers, providing for an acid-labile immuno conjugate wherein the drug may be released from its antibody conjugated part in an acidic, e.g. tumoural or environment
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/56—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
- A61K47/59—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes
- A61K47/605—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes the macromolecule containing phosphorus in the main chain, e.g. poly-phosphazene
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/545—Heterocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/56—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
- A61K47/59—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6801—Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
- A61K47/6851—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Definitions
- ADCs Antibody-drug conjugates
- ADCs are one class of targeted drug conjugates that are of particular interest for cancer treatment.
- ADCs combine the targeting features of monoclonal antibodies with cancer-killing ability of cytotoxic agents to provide a therapeutic with several advantages over other chemotherapeutics.
- challenges related to the complexity of ADC constructs, specifically the chemical linker between antibody and drug has caused significant difficulties for development of new and effective therapeutics.
- Adcetris® and Kadcyla® are commercially available globally (Zevalin® has been approved in China only). Pioneers Pfizer/Wyeth withdrew Mylotarg® in 2010 after safety issues were observed during a comparative clinical trial.
- isotopes that can be incorporated into the disclosed compounds include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine, chlorine, and iodine, such as 2 H, 3 H, U C, 13 C, 14 C, 13 N, 15 N, 15 0, 17 0, 18 0, 31 P, 32 P, 35 S, 18 F, 36 C1, 123 I, and 125 I, respectively.
- methotrexate platinum analogs such as cisplatin and carboplatin; vinblastine; platinum; etoposide (VP- 16); ifosfamide; mitomycin C; mitoxantrone; vincristine; vinorelbine; navelbine; novantrone; teniposide; daunomycin; aminopterin; xeloda; ibandronate; camptothecin-11 (CPT-11); topoisomeRASe inhibitor RFS 2000;
- the compounds of the invention are administered in dosages. It is known in the art that due to intersubject variability in compound pharmacokinetics, individualization of dosing regimen is necessary for optimal therapy. Dosing for a compound of the invention may be found by routine experimentation in light of the instant disclosure.
- compositions optionally include other medicinal or pharmaceutical agents, carriers, adjuvants, such as preserving, stabilizing, wetting or emulsifying agents, solution promoters, salts for regulating the osmotic pressure, buffers, and/or other therapeutically valuable substances.
- adjuvants such as preserving, stabilizing, wetting or emulsifying agents, solution promoters, salts for regulating the osmotic pressure, buffers, and/or other therapeutically valuable substances.
- poly(methylmethacrylate), polyacrylamide, polycarbophil, acrylic acid/butyl acrylate copolymer, sodium alginate and dextran are examples of poly(methylmethacrylate), polyacrylamide, polycarbophil, acrylic acid/butyl acrylate copolymer, sodium alginate and dextran.
- Useful pharmaceutical compositions also, optionally, include solubilizing agents to aid in the solubility of a compound of structure (I).
- solubilizing agent generally includes agents that result in formation of a micellar solution or a true solution of the agent.
- Certain acceptable nonionic surfactants for example polysorbate 80, are useful as solubilizing agents, as can ophthalmically acceptable glycols, polyglycols, e.g., polyethylene glycol 400, and glycol ethers.
- useful pharmaceutical compositions optionally include one or more pH adjusting agents or buffering agents, including acids such as acetic, boric, citric, lactic, phosphoric and hydrochloric acids; bases such as sodium hydroxide, sodium phosphate, sodium borate, sodium citrate, sodium acetate, sodium lactate and tris-hydroxymethylaminomethane; and buffers such as citrate/dextrose, sodium bicarbonate and ammonium chloride.
- acids such as acetic, boric, citric, lactic, phosphoric and hydrochloric acids
- bases such as sodium hydroxide, sodium phosphate, sodium borate, sodium citrate, sodium acetate, sodium lactate and tris-hydroxymethylaminomethane
- buffers such as citrate/dextrose, sodium bicarbonate and ammonium chloride.
- acids, bases and buffers are included in an amount required to maintain pH of the composition in an acceptable range.
- cetyltrimethylammonium bromide and cetylpyridinium chloride are examples of cetyltrimethylammonium bromide and cetylpyridinium chloride.
- lymphoma prostate cancer, rectal cancer, transitional cell cancer, retinoblastoma, rhabdomyosarcoma, salivary gland cancer, skin cancer, stomach (gastric) cancer, small cell lung cancer, small intestine cancer, soft tissue sarcoma, T-Cell lymphoma, testicular cancer, throat cancer, thymoma and thymic carcinoma, thyroid cancer, transitional cell cancer of the renal pelvis and ureter, trophoblastic tumor, unusual cancers of childhood, urethral cancer, uterine sarcoma, vaginal cancer, vulvar cancer, or Viral-Induced cancer.
- the analyte molecule is a nucleic acid, amino acid or a polymer thereof (e.g., polynucleotide or polypeptide). In still more embodiments, the analyte molecule is an enzyme, receptor, receptor ligand, antibody, glycoprotein, aptamer or prion.
- Suitable protecting groups include hydroxy, amino, mercapto and carboxylic acid.
- Suitable protecting groups for hydroxy include trialkylsilyl or diarylalkylsilyl (for example, t-butyldimethylsilyl, t-butyldiphenylsilyl or trimethylsilyl), tetrahydropyranyl, benzyl, and the like.
- Suitable protecting groups for amino, amidino and guanidino include t-butoxycarbonyl, benzyloxycarbonyl, and the like.
- Ibuprofen-NHS was reacted with 2-1 (2-amino- 1,3 -propane diol) followed by the addition of a trityl protecting group to afford intermediate 2-3.
- the protected product 2-3 was then reacted with 2-4 to afford the final product, 2-5 ibuprofen-phosphoramidite (79%).
- the ibuprofen- phosphoramidite was then used for automated DNA synthesis to incorporate ibuprofen as a representative biologically active moiety into embodiments of the compounds described herein.
- the composition of the dendrimer backbone can also be selected to afford desirable solubility properties, for example, by controlling the incorporation of charged moieties (e.g., number, frequency, spacing, etc.).
- the side chains can be selected to provide a source for tuning the solubility of the compounds disclosed herein. For example, providing positively charged moieties to interact with nucleic acid oligomers to aid in transport across cell membranes.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Cell Biology (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020207006070A KR20200064059A (ko) | 2017-10-05 | 2018-10-05 | 프로그램가능한 수지상 약물 |
| US16/639,499 US12290571B2 (en) | 2017-10-05 | 2018-10-05 | Programmable dendritic drugs |
| EP18792814.8A EP3691689A1 (en) | 2017-10-05 | 2018-10-05 | Programmable dendritic drugs |
| JP2020508523A JP7403744B2 (ja) | 2017-10-05 | 2018-10-05 | プログラマブルな樹枝状薬物 |
| CN201880056126.7A CN111093711A (zh) | 2017-10-05 | 2018-10-05 | 可编程的树枝状药物 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762568681P | 2017-10-05 | 2017-10-05 | |
| US62/568,681 | 2017-10-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2019071153A1 true WO2019071153A1 (en) | 2019-04-11 |
Family
ID=63963607
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2018/054648 Ceased WO2019071153A1 (en) | 2017-10-05 | 2018-10-05 | PROGRAMMABLE DENDRITIC MEDICINES |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US12290571B2 (https=) |
| EP (1) | EP3691689A1 (https=) |
| JP (1) | JP7403744B2 (https=) |
| KR (1) | KR20200064059A (https=) |
| CN (1) | CN111093711A (https=) |
| WO (1) | WO2019071153A1 (https=) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10844228B2 (en) | 2018-03-30 | 2020-11-24 | Becton, Dickinson And Company | Water-soluble polymeric dyes having pendant chromophores |
| WO2021113651A3 (en) * | 2019-12-04 | 2021-08-26 | Ashvattha Therapeutics, Inc. | Dendrimer compositions and methods for drug delivery |
| CN115702007A (zh) * | 2020-06-01 | 2023-02-14 | Bik治疗公司 | 具有提高的药物递送和内化效率的药物偶联物 |
| US11931418B2 (en) | 2020-04-24 | 2024-03-19 | Ashvattha Therapeutics, Inc. | Methods of treating severe inflammation |
| US12180401B2 (en) | 2021-04-07 | 2024-12-31 | Becton, Dickinson And Company | Water-soluble fluorescent polymeric dyes |
Families Citing this family (26)
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| EP3019559A4 (en) | 2013-08-22 | 2017-04-05 | Sony Corporation | Water soluble fluorescent or colored dyes and methods for their use |
| KR102646956B1 (ko) | 2015-02-26 | 2024-03-14 | 소니그룹주식회사 | 페닐에티닐나프탈렌 염료 및 이의 사용 방법 |
| US11827661B2 (en) | 2015-02-26 | 2023-11-28 | Sony Group Corporation | Water soluble fluorescent or colored dyes comprising conjugating groups |
| CN107709470B (zh) | 2015-05-11 | 2021-01-29 | 索尼公司 | 超亮二聚或多聚染料 |
| AU2017240154B2 (en) | 2016-04-01 | 2021-08-12 | Sony Group Corporation | Ultra bright dimeric or polymeric dyes |
| CN109415574B (zh) | 2016-04-01 | 2021-05-28 | 索尼公司 | 具有刚性间隔基团的超亮二聚体或聚合物染料 |
| WO2017177065A2 (en) | 2016-04-06 | 2017-10-12 | Sony Corporation | Ultra bright dimeric or polymeric dyes with spacing linker groups |
| JP7527537B2 (ja) | 2016-05-10 | 2024-08-05 | ソニーグループ株式会社 | ペプチド骨格を有する超明色ポリマー染料 |
| EP3455299B1 (en) | 2016-05-10 | 2024-01-17 | Sony Group Corporation | Compositions comprising a polymeric dye and a cyclodextrin and uses thereof |
| EP3455300A1 (en) | 2016-05-11 | 2019-03-20 | Sony Corporation | Ultra bright dimeric or polymeric dyes |
| EP3464477A1 (en) | 2016-06-06 | 2019-04-10 | Sony Corporation | Ionic polymers comprising fluorescent or colored reporter groups |
| JP7312929B2 (ja) | 2016-07-29 | 2023-07-24 | ソニーグループ株式会社 | 超明色二量体またはポリマー色素およびその調製のための方法 |
| KR20260011205A (ko) | 2017-10-05 | 2026-01-22 | 소니그룹주식회사 | 프로그램가능한 중합체성 약물 |
| CN111836645A (zh) | 2017-11-16 | 2020-10-27 | 索尼公司 | 可编程的聚合药物 |
| CN111565756A (zh) | 2018-01-12 | 2020-08-21 | 索尼公司 | 包含生物活性化合物的具有刚性间隔基团的聚合物 |
| US12539334B2 (en) | 2018-01-12 | 2026-02-03 | Sony Group Corporation | Phosphoalkyl polymers comprising biologically active agents |
| EP3737417B1 (en) | 2018-01-12 | 2025-08-27 | Sony Group Corporation | Phosphoalkyl ribose polymers comprising biologically active compounds |
| KR102742386B1 (ko) | 2018-03-19 | 2024-12-16 | 소니그룹주식회사 | 형광 신호 향상을 위한 2가 금속의 사용 |
| CN118480073A (zh) | 2018-03-21 | 2024-08-13 | 索尼公司 | 具有连接体基团的聚合串联染料 |
| JP7580689B2 (ja) | 2018-06-27 | 2024-11-12 | ソニーグループ株式会社 | デオキシリボースを含むリンカー基を有するポリマー色素 |
| KR20210032434A (ko) | 2018-07-13 | 2021-03-24 | 소니 주식회사 | 유기인산염 단위를 포함하는 백본을 갖는 중합체성 염료 |
| EP3952916A1 (en) * | 2019-04-11 | 2022-02-16 | Sony Group Corporation | Programmable polymeric drugs |
| WO2021062176A2 (en) | 2019-09-26 | 2021-04-01 | Sony Corporation | Polymeric tandem dyes with linker groups |
| EP4038081A1 (en) | 2019-09-30 | 2022-08-10 | Sony Group Corporation | Nucleotide probes |
| CN111521593B (zh) * | 2020-05-12 | 2021-05-11 | 中国农业大学 | 一种基于水溶性苝酰亚胺衍生物的快速可视化检测方法 |
| EP4256078A1 (en) | 2020-12-07 | 2023-10-11 | Sony Group Corporation | Spacing linker group design for brightness enhancement in dimeric or polymeric dyes |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009132020A2 (en) * | 2008-04-21 | 2009-10-29 | The Regents Of The University Of California | Selective high-affinity polydentate ligands and methods of making such |
| WO2015027176A1 (en) | 2013-08-22 | 2015-02-26 | Sony Corporation | Water soluble fluorescent or colored dyes and methods for their use |
| WO2016138461A1 (en) | 2015-02-26 | 2016-09-01 | Sony Corporation | Water soluble fluorescent or colored dyes comprising conjugating groups |
| WO2016183185A1 (en) | 2015-05-11 | 2016-11-17 | Sony Corporation | Ultra bright dimeric or polymeric dyes |
Family Cites Families (173)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4450305A (en) | 1982-10-25 | 1984-05-22 | American Cyanamid Company | Poly(ethyleneoxy)-substituted-9,10-bis(phenylethynyl)anthracenes |
| US4476229A (en) | 1982-11-08 | 1984-10-09 | Abbott Laboratories | Substituted carboxyfluoresceins |
| SU1121931A1 (ru) | 1983-01-10 | 1988-04-15 | Институт Биологической Химии Ан Бсср | Конъюгаты тиреоидных гормонов с альбумином дл выработки антител к тиреоидным гормонам у животных |
| EP0355864A3 (en) | 1984-03-15 | 1991-09-18 | Wako Pure Chemical Industries, Ltd. | Method of quantitatively measuring an oxidative substance by using triphenyl methane type leuco compounds as coloring matter |
| JPH0665677B2 (ja) | 1985-03-09 | 1994-08-24 | 三菱化成株式会社 | リン脂質類似構造を有するジオ−ルおよびその製造方法 |
| US5268486A (en) | 1986-04-18 | 1993-12-07 | Carnegie-Mellon Unversity | Method for labeling and detecting materials employing arylsulfonate cyanine dyes |
| US5053054A (en) | 1988-09-12 | 1991-10-01 | Ortho Pharmaceutical Corporation | Methods and reagents for staining intracellular components |
| US5318894A (en) | 1990-01-30 | 1994-06-07 | Miles Inc. | Composition, device and method of assaying for peroxidatively active substances |
| US6365730B1 (en) | 1990-06-19 | 2002-04-02 | Gene Shears Pty. Limited | DNA-Armed ribozymes and minizymes |
| JPH04282391A (ja) | 1991-03-08 | 1992-10-07 | Fujisawa Pharmaceut Co Ltd | エタノールアミン誘導体およびその製造法 |
| US5698391A (en) | 1991-08-23 | 1997-12-16 | Isis Pharmaceuticals, Inc. | Methods for synthetic unrandomization of oligomer fragments |
| CA2119126C (en) | 1991-09-16 | 1996-09-03 | Molecular Probes, Inc. | Dimers of unsymmetrical cyanine dyes |
| EP1067134B1 (en) | 1991-11-07 | 2004-07-28 | Nanotronics, Inc. | Hybridization of polynucleotides conjugated with chromophores and fluorophores to generate donor-to-donor energy transfer system |
| EP0693065B1 (en) | 1993-04-13 | 2001-12-05 | Naxcor | Non-nucleosidic coumarin derivatives as polynucleotide-crosslinking agents |
| EP0708837B1 (en) | 1993-07-13 | 2006-03-08 | Abbott Laboratories | Fluorescent polymer labeled conjugates and intermediates |
| ATE227342T1 (de) | 1993-09-02 | 2002-11-15 | Ribozyme Pharm Inc | Enzymatische nukleiksaüre die nicht-nukleotide enthaltet |
| US5886177A (en) | 1994-01-11 | 1999-03-23 | Isis Pharmaceuticals, Inc. | Phosphate linked oligomers |
| US6171859B1 (en) | 1994-03-30 | 2001-01-09 | Mitokor | Method of targeting conjugate molecules to mitochondria |
| US5994143A (en) | 1996-02-01 | 1999-11-30 | Abbott Laboratories | Polymeric fluorophores enhanced by moieties providing a hydrophobic and conformationally restrictive microenvironment |
| US6218108B1 (en) | 1997-05-16 | 2001-04-17 | Research Corporation Technologies, Inc. | Nucleoside analogs with polycyclic aromatic groups attached, methods of synthesis and uses therefor |
| DE19633268A1 (de) | 1996-08-19 | 1998-02-26 | Hoechst Ag | Polymere Gallensäure-Resorptionsinhibitoren mit gleichzeitiger Gallensäure-Adsorberwirkung |
| JP2001511128A (ja) | 1997-01-28 | 2001-08-07 | ファルマシア・アンド・アップジョン・カンパニー | 水不溶性ポルフィリンの脂質錯体の凍結乾燥物 |
| US6893868B2 (en) | 1997-02-20 | 2005-05-17 | Onco Immunin, Inc. | Homo-doubly labeled compositions for the detection of enzyme activity in biological samples |
| US5986030A (en) | 1997-04-15 | 1999-11-16 | Nalco Chemical Company | Fluorescent water soluble polymers |
| DE19717904A1 (de) | 1997-04-23 | 1998-10-29 | Diagnostikforschung Inst | Säurelabile und enzymatisch spaltbare Farbstoffkonstrukte zur Diagnostik mit Nahinfrarotlicht und zur Therapie |
| JP3078793B2 (ja) | 1998-04-30 | 2000-08-21 | 株式会社分子バイオホトニクス研究所 | ロタキサン構造を有する色素、ラベル化剤、およびラベル化方法 |
| US7060708B2 (en) | 1999-03-10 | 2006-06-13 | New River Pharmaceuticals Inc. | Active agent delivery systems and methods for protecting and administering active agents |
| US6716452B1 (en) | 2000-08-22 | 2004-04-06 | New River Pharmaceuticals Inc. | Active agent delivery systems and methods for protecting and administering active agents |
| US6627400B1 (en) | 1999-04-30 | 2003-09-30 | Aclara Biosciences, Inc. | Multiplexed measurement of membrane protein populations |
| US6514700B1 (en) | 1999-04-30 | 2003-02-04 | Aclara Biosciences, Inc. | Nucleic acid detection using degradation of a tagged sequence |
| US20020142329A1 (en) | 1999-04-30 | 2002-10-03 | Aclara Biosciences, Inc. | Compositions and methods employing cleavable electrophoretic tag reagents |
| US7037654B2 (en) | 1999-04-30 | 2006-05-02 | Aclara Biosciences, Inc. | Methods and compositions for enhancing detection in determinations employing cleavable electrophoretic tag reagents |
| WO2001007430A1 (en) | 1999-07-22 | 2001-02-01 | Nalco Chemical Compant | Fluorescent water-soluble polymers |
| US6479650B1 (en) | 1999-12-14 | 2002-11-12 | Research Corporation Technologies, Inc. | Fluorescent nucleoside analogs and combinatorial fluorophore arrays comprising same |
| AU2001245643A1 (en) | 2000-03-14 | 2001-09-24 | Genigma Corporation | Biomarkers for the labeling, visual detection and quantification of biomolecules |
| CA2402955C (en) | 2000-03-28 | 2010-03-09 | Nanosphere, Inc. | Nanoparticles having oligonucleotides attached thereto and uses therefor |
| US20040067498A1 (en) | 2000-04-28 | 2004-04-08 | Ahmed Chenna | Detection of nucleic acid sequences by cleavage and separation of tag-containing structures |
| AU6299401A (en) | 2000-05-08 | 2001-11-20 | Qtl Biosystems Llc | Improvements to the fluorescent polymer-qtl approach to biosensing |
| US6852709B2 (en) | 2000-05-31 | 2005-02-08 | Johns Hopkins University | Biologically useful polyphosphates |
| US20020099013A1 (en) | 2000-11-14 | 2002-07-25 | Thomas Piccariello | Active agent delivery systems and methods for protecting and administering active agents |
| CA2421582A1 (en) | 2000-09-11 | 2002-03-21 | The Trustees Of Columbia University In The City Of New York | Combinatorial fluorescence energy transfer tags and uses thereof |
| DE60116510T2 (de) | 2000-09-19 | 2006-07-13 | Li-Cor, Inc., Lincoln | Cyaninfarbstoffe |
| US6448407B1 (en) | 2000-11-01 | 2002-09-10 | Pe Corporation (Ny) | Atropisomers of asymmetric xanthene fluorescent dyes and methods of DNA sequencing and fragment analysis |
| US8394813B2 (en) | 2000-11-14 | 2013-03-12 | Shire Llc | Active agent delivery systems and methods for protecting and administering active agents |
| GB2372256A (en) | 2001-02-14 | 2002-08-21 | Kalibrant Ltd | Detectable entity comprising a plurality of detectable units releasably connected together by stimulus-cleavable linkers for use in fluorescence detection |
| US6743905B2 (en) | 2001-04-16 | 2004-06-01 | Applera Corporation | Mobility-modified nucleobase polymers and methods of using same |
| US8323903B2 (en) | 2001-10-12 | 2012-12-04 | Life Technologies Corporation | Antibody complexes and methods for immunolabeling |
| JP3813890B2 (ja) | 2002-03-22 | 2006-08-23 | 富士写真フイルム株式会社 | 3層レジストプロセス用中間層材料組成物及びそれを用いたパターン形成方法 |
| US20040086914A1 (en) | 2002-07-12 | 2004-05-06 | Affymetrix, Inc. | Nucleic acid labeling methods |
| US6806523B2 (en) * | 2002-07-15 | 2004-10-19 | Micron Technology, Inc. | Magnetoresistive memory devices |
| AU2003262833A1 (en) | 2002-08-23 | 2004-03-11 | The Board Of Trustees Of The Leland Stanford Junior University | Fluorescent glycosides and methods for their use |
| KR20050055717A (ko) | 2002-08-26 | 2005-06-13 | 더 리전츠 오브 더 유니버시티 오브 캘리포니아 | 집광 다발색단을 사용하여 폴리뉴클레오티드를 검출 및 분석하기 위한 방법 및 조성물 |
| US20040138467A1 (en) | 2002-11-26 | 2004-07-15 | French Roger Harquail | Aromatic and aromatic/heteroaromatic molecular structures with controllable electron conducting properties |
| US7759459B2 (en) | 2003-01-10 | 2010-07-20 | Albert Einstein College Of Medicine Of Yeshiva University | Fluorescent assays for protein kinases |
| US7238792B2 (en) | 2003-03-18 | 2007-07-03 | Washington State University Research Foundation | Foldable polymers as probes |
| US7172907B2 (en) | 2003-03-21 | 2007-02-06 | Ge Healthcare Bio-Sciences Corp. | Cyanine dye labelling reagents with meso-substitution |
| DE602004022056D1 (de) | 2003-08-14 | 2009-08-27 | Diatos | Antibakterielle zusammensetzung, vor allem zur bekämpfung gramnegativer bakterien, umfassend ein peptid und ein vorteilhafterweise hydrophobes antibakterielles agens |
| EP1689764B1 (en) | 2003-11-19 | 2013-01-02 | AlleLogic Biosciences Corporation | Oligonucleotides labeled with a plurality of fluorophores |
| AU2003296419A1 (en) | 2003-12-09 | 2005-07-21 | Molecular Probes, Inc. | Pyrenyloxysulfonic acid fluorescent agents |
| EP1768998A2 (en) | 2004-04-27 | 2007-04-04 | Alnylam Pharmaceuticals Inc. | Single-stranded and double-stranded oligonucleotides comprising a 2-arylpropyl moiety |
| US20060035302A1 (en) | 2004-06-21 | 2006-02-16 | Applera Corporation | Kinase substrates with multiple phosphorylation sites |
| JP5214967B2 (ja) | 2004-08-13 | 2013-06-19 | エポック バイオサイエンシズ インコーポレーティッド | ホスホン酸蛍光色素および複合体 |
| EP1789794A1 (en) | 2004-09-14 | 2007-05-30 | Applera Corporation, Applied Biosystems Group | Multi-chromophoric quencher constructs for use in high sensitivity energy transfer probes |
| US8153706B2 (en) | 2004-10-25 | 2012-04-10 | Hewlett-Packard Development Company, L.P. | Polymeric colorants having pigment and dye components and corresponding ink compositions |
| PL1655317T3 (pl) | 2004-11-09 | 2007-10-31 | Ipagsa Ind Sl | Termoreaktywne polimery absorbujące promieniowanie podczerwone i ich zastosowanie w termoczułej litograficznej płycie drukarskiej |
| US7897684B2 (en) | 2005-01-10 | 2011-03-01 | The Regents Of The University Of California | Conjugated polymers suitable for strand-specific polynucleotide detection in homogeneous and solid state assays |
| CA2599709A1 (en) | 2005-03-09 | 2006-09-21 | Cepheid | Polar dyes |
| US8227621B2 (en) | 2005-06-30 | 2012-07-24 | Li-Cor, Inc. | Cyanine dyes and methods of use |
| WO2007038659A1 (en) | 2005-09-26 | 2007-04-05 | Invitrogen Corporation | Violet laser excitable dyes and their method of use |
| CN101360997B (zh) | 2005-11-18 | 2013-05-01 | 美国政府健康及人类服务部,疾病控制和预防中心 | 改性心磷脂及其应用 |
| JP5410760B2 (ja) | 2005-12-12 | 2014-02-05 | チバ ホールディング インコーポレーテッド | 半導体素子、化合物、半導体素子の半導体層及び薄膜トランジスタ素子を作製する方法 |
| US20070148094A1 (en) | 2005-12-22 | 2007-06-28 | Uzgiris Egidijus E | Polymeric imaging agents and medical imaging methods |
| WO2007094135A1 (ja) | 2006-02-15 | 2007-08-23 | Gifu University | オリゴヌクレオチド誘導体及びその利用 |
| ES2369608T3 (es) | 2006-04-13 | 2011-12-02 | Midatech Ltd. | Nanopartículas que contienen tres ligandos diferentes para proporcionar respuestas inmunitarias frente a agentes infecciosos. |
| EP2054770A2 (en) | 2006-08-12 | 2009-05-06 | STX Aprilis, Inc. | Sensitizer dyes for photoacid generating systems using short visible wavelengths |
| CN101523631B (zh) | 2006-10-12 | 2010-09-22 | 出光兴产株式会社 | 有机薄膜晶体管元件以及有机薄膜发光晶体管 |
| WO2008076524A2 (en) | 2006-10-27 | 2008-06-26 | Life Technologies Corporation | Fluorogenic ph sensitive dyes and their method of use |
| US8053588B2 (en) | 2007-03-07 | 2011-11-08 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Organosilane compound and organosilica obtained therefrom |
| US9556210B2 (en) | 2007-04-23 | 2017-01-31 | Sabag-Rfa Ltd. | System for delivering therapeutic agents into living cells and cells nuclei |
| EP2144633B1 (en) | 2007-04-23 | 2014-07-16 | Deliversir Ltd | A system for delivering therapeutic agents into living cells and cells nuclei |
| US9156865B2 (en) | 2007-04-23 | 2015-10-13 | Deliversir Ltd | System for delivering therapeutic agents into living cells and cells nuclei |
| EP2155805A2 (en) | 2007-05-11 | 2010-02-24 | Basf Se | Polymeric dyes |
| EP2014698A1 (en) | 2007-07-12 | 2009-01-14 | Crystax Pharmaceuticals S.L. | Polymers and their use as fluorescent labels |
| TWI409280B (zh) | 2007-07-31 | 2013-09-21 | American Dye Source Inc | 聚合物染料、塗覆層組合物及熱微影印刷板 |
| GB2456298A (en) | 2008-01-07 | 2009-07-15 | Anthony Ian Newman | Electroluminescent materials comprising oxidation resistant fluorenes |
| KR101564796B1 (ko) | 2008-03-10 | 2015-10-30 | 고쿠리츠다이가쿠호우진 도쿄다이가쿠 | 비하전성 친수성 블록 및 측사슬의 일부에 소수성 기가 도입된 카티온성 폴리아미노산 블록을 포함하여 이루어지는 공중합체, 그 사용 |
| KR101041446B1 (ko) | 2008-07-21 | 2011-06-14 | 부산대학교 산학협력단 | 공액고분자 2단계 fret 시스템 및 바이오센서 |
| JPWO2010026957A1 (ja) | 2008-09-03 | 2012-02-02 | 国立大学法人富山大学 | 水溶性ロタキサン型蛍光色素および蛍光性有機分子 |
| EP2366785B1 (en) | 2008-11-14 | 2013-01-16 | Japan Science And Technology Agency | Oligonucleotide derivative, labeling agent, and use of the labeling agent |
| JP5798487B2 (ja) | 2008-11-20 | 2015-10-21 | ネーデルランドセ・オルガニサティ・フォール・トゥーヘパスト−ナトゥールウェテンスハッペライク・オンデルズーク・テーエヌオー | Fretに基づく病原体の迅速診断 |
| CA2745307A1 (en) | 2008-12-12 | 2010-06-17 | University Of Massachusetts | Polyesters with grafted zwitterions |
| CN106519588B (zh) | 2009-11-09 | 2019-08-20 | 华盛顿大学商业化中心 | 官能化发色聚合物点及其生物共轭体 |
| US9400273B1 (en) | 2009-12-09 | 2016-07-26 | Life Technologies Corporation | 7-hydroxycoumarin-based cell-tracking reagents |
| US9221759B2 (en) | 2010-01-13 | 2015-12-29 | Rutgers, The State University Of New Jersey | Fluorophore chelated lanthanide luminescent probes with improved quantum efficiency |
| EP2545373B1 (en) | 2010-03-11 | 2022-08-24 | Medtronic Minimed, Inc. | Measuring analyte concentration incorporating temperature and ph correction |
| EP2553019A1 (en) | 2010-03-26 | 2013-02-06 | Mersana Therapeutics, Inc. | Modified polymers for delivery of polynucleotides, method of manufacture, and methods of use thereof |
| WO2011150079A1 (en) | 2010-05-25 | 2011-12-01 | Carnegie Mellon University | Targeted probes of cellular physiology |
| JPWO2012005310A1 (ja) | 2010-07-08 | 2013-09-05 | 旭硝子株式会社 | 含フッ素芳香族化合物、有機半導体材料および有機薄膜デバイス |
| WO2012039855A1 (en) | 2010-09-22 | 2012-03-29 | The Board Of Regents Of The University Of Texas System | Ph-sensitive compositions for delivery of beta lapachone and methods of use |
| CA3065178C (en) | 2010-12-13 | 2022-02-01 | Quiapeg Pharmaceuticals Ab | Functionalized polymers |
| WO2012086857A1 (ko) | 2010-12-21 | 2012-06-28 | (주)파낙스이엠 | 광역학 진단 또는 치료를 위한 결합체 및 이의 제조방법 |
| CN102174078A (zh) | 2011-01-10 | 2011-09-07 | 中国药科大学 | 肿瘤细胞选择性穿膜肽的应用 |
| WO2013012687A2 (en) | 2011-07-15 | 2013-01-24 | Glumetrics, Inc. | Combinations of fluorphores and pyridinium boronic acid quenchers for use in analyte sensors |
| JP2014527071A (ja) | 2011-08-31 | 2014-10-09 | マリンクロッド エルエルシー | H−ホスホネートによるナノ粒子pegの改変 |
| US20130059343A1 (en) | 2011-09-06 | 2013-03-07 | Li-Cor, Inc. | Nucleotide derivatives |
| US9085761B1 (en) | 2012-06-14 | 2015-07-21 | Affymetrix, Inc. | Methods and compositions for amplification of nucleic acids |
| EP2895607B1 (en) | 2012-09-12 | 2021-05-05 | Quark Pharmaceuticals, Inc. | Double-stranded oligonucleotide molecules to ddit4 and methods of use thereof |
| WO2014055253A1 (en) | 2012-10-04 | 2014-04-10 | The General Hospital Corporation | Methods of synthesizing and using peg-like fluorochromes |
| AU2013336237A1 (en) | 2012-10-22 | 2015-06-11 | Sabag-Rfa Ltd | A system for delivering therapeutic agents into living cells and cells nuclei |
| WO2014102806A1 (en) | 2012-12-31 | 2014-07-03 | Yeda Research And Development Co. Ltd. | Protein biosensors, cross reactive sensor arrays and methods of use thereof |
| US9545447B2 (en) | 2013-01-04 | 2017-01-17 | The Texas A&M University System | Polymer-drug systems |
| US9169256B2 (en) | 2013-03-13 | 2015-10-27 | Elitechgroup B.V. | Artificial nucleic acids |
| WO2014159392A1 (en) | 2013-03-14 | 2014-10-02 | Dana-Farber Cancer Institute, Inc. | Bromodomain binding reagents and uses thereof |
| CA2901379C (en) | 2013-03-15 | 2023-05-16 | Visen Medical, Inc. | Substituted silaxanthenium red to near-infrared fluorochromes for in vitro and in vivo imaging and detection |
| WO2014147642A1 (en) | 2013-03-19 | 2014-09-25 | Council Of Scientific & Industrial Research | Substituted fluoranthene-7-carbonitriles as fluorescent dyes for cell imaging applications |
| CN103319378B (zh) | 2013-06-27 | 2015-06-10 | 中国科学院宁波材料技术与工程研究所 | 两性离子有机小分子太阳能电池阴极界面材料及其制法和用途 |
| KR101572901B1 (ko) | 2013-07-12 | 2015-12-15 | 부산대학교 산학협력단 | 2-단계 fret를 이용한 공액고분자 전해질 및 압타머 프로브 기반 표적 물질의 검출 방법 및 형광 센서 |
| TWI603305B (zh) * | 2013-09-27 | 2017-10-21 | 鴻海精密工業股份有限公司 | 顯示裝置、拼接式顯示器及顯示面板 |
| US10406246B2 (en) | 2013-10-17 | 2019-09-10 | Deutsches Kresbsforschungszentrum | Double-labeled probe for molecular imaging and use thereof |
| WO2015068697A1 (ja) | 2013-11-11 | 2015-05-14 | オリンパスメディカルシステムズ株式会社 | 処置システム |
| WO2015085204A1 (en) | 2013-12-06 | 2015-06-11 | Monosol Llc | Fluorescent tracer for water-soluble films, related methods, and related articles |
| CN105917226B (zh) * | 2013-12-20 | 2018-06-01 | 豪夫迈·罗氏有限公司 | 包含两个或多个疏水结构域和一个含有peg部分的亲水结构域的化合物用于稳定细胞的用途 |
| KR101829159B1 (ko) | 2014-01-16 | 2018-02-13 | 소니 주식회사 | 수용성 형광 또는 유색 염료 |
| JP6374172B2 (ja) | 2014-01-31 | 2018-08-15 | 富士フイルム株式会社 | 着色組成物、およびこれを用いた硬化膜、カラーフィルタ、パターン形成方法、カラーフィルタの製造方法、固体撮像素子、画像表示装置ならびに染料多量体 |
| CN104072727A (zh) | 2014-06-23 | 2014-10-01 | 华南理工大学 | 一种含磷脂酰胆碱基的2,7-芴的共轭聚合物及其制备方法与应用 |
| AU2015329625B2 (en) | 2014-10-10 | 2018-04-05 | Pfizer Inc. | Synergistic auristatin combinations |
| US10709791B2 (en) | 2014-11-12 | 2020-07-14 | University Of Washington | Stabilized polymeric carriers for therapeutic agent delivery |
| EP3218414A1 (en) | 2014-11-14 | 2017-09-20 | Angiochem Inc. | Conjugates including an antibody moiety, a polypeptide that traverses the blood-brain barrier, and a cytotoxin |
| DK178808B1 (en) | 2014-12-12 | 2017-02-13 | Envision Energy Denmark Aps | Floating wind turbine structure with reduced tower height and method for optimising the weight thereof |
| KR102646956B1 (ko) | 2015-02-26 | 2024-03-14 | 소니그룹주식회사 | 페닐에티닐나프탈렌 염료 및 이의 사용 방법 |
| WO2016144652A1 (en) | 2015-03-12 | 2016-09-15 | Becton, Dickinson And Company | Polymeric bodipy dyes and methods for using the same |
| US9670318B2 (en) | 2015-05-28 | 2017-06-06 | Miltenyi Biotec Gmbh | Bright fluorochromes based on multimerization of fluorescent dyes |
| US11512160B2 (en) | 2015-06-02 | 2022-11-29 | University Of Washington | Free-standing non-fouling polymers, their compositions, and related monomers |
| JP6817288B2 (ja) | 2015-08-10 | 2021-01-20 | ハンジョウ ディーエーシー バイオテック シーオー.,エルティディ.Hangzhou Dac Biotech Co.,Ltd. | 新規な連結体及び生体分子と薬物との特異的共役におけるその使用 |
| US9691615B2 (en) * | 2015-08-28 | 2017-06-27 | International Business Machines Corporation | Chemoepitaxy-based directed self assembly process with tone inversion for unidirectional wiring |
| US11510993B2 (en) | 2015-10-06 | 2022-11-29 | Merck Sharp & Dohme Llc | Antibody drug conjugate for anti-inflammatory applications |
| AU2016359230B2 (en) | 2015-11-25 | 2020-04-23 | Ligachem Biosciences Inc. | Conjugates comprising self-immolative groups and methods related thereto |
| CN108368509B (zh) * | 2015-12-04 | 2022-03-22 | 全药工业株式会社 | 改善了血中滞留性的抗il-17适体 |
| US9913992B2 (en) | 2015-12-22 | 2018-03-13 | Colgate-Palmolive Company | Oral treatment device |
| JP2017124994A (ja) | 2016-01-15 | 2017-07-20 | 靖彦 中村 | 癌治療及び癌再発防止のための装置並びにポルフィリン類含有製剤 |
| CN109415574B (zh) | 2016-04-01 | 2021-05-28 | 索尼公司 | 具有刚性间隔基团的超亮二聚体或聚合物染料 |
| AU2017240154B2 (en) | 2016-04-01 | 2021-08-12 | Sony Group Corporation | Ultra bright dimeric or polymeric dyes |
| WO2017177065A2 (en) | 2016-04-06 | 2017-10-12 | Sony Corporation | Ultra bright dimeric or polymeric dyes with spacing linker groups |
| JP7527537B2 (ja) | 2016-05-10 | 2024-08-05 | ソニーグループ株式会社 | ペプチド骨格を有する超明色ポリマー染料 |
| EP3455299B1 (en) | 2016-05-10 | 2024-01-17 | Sony Group Corporation | Compositions comprising a polymeric dye and a cyclodextrin and uses thereof |
| EP3455300A1 (en) | 2016-05-11 | 2019-03-20 | Sony Corporation | Ultra bright dimeric or polymeric dyes |
| EP3464477A1 (en) | 2016-06-06 | 2019-04-10 | Sony Corporation | Ionic polymers comprising fluorescent or colored reporter groups |
| JP7312929B2 (ja) | 2016-07-29 | 2023-07-24 | ソニーグループ株式会社 | 超明色二量体またはポリマー色素およびその調製のための方法 |
| US20180092993A1 (en) | 2016-09-01 | 2018-04-05 | Life Technologies Corporation | Compositions and methods for enhanced fluorescence |
| GB2554666B (en) | 2016-09-30 | 2019-12-18 | Sumitomo Chemical Co | Composite Particle |
| CN106589005B (zh) | 2016-11-01 | 2019-08-06 | 北京擎科生物科技有限公司 | 一种荧光信号放大探针中间体、荧光探针及其制备方法 |
| AU2018223809B2 (en) | 2017-02-27 | 2022-12-15 | Ivanti, Inc. | Systems and methods for role-based computer security configurations |
| US12398104B2 (en) | 2017-04-27 | 2025-08-26 | The Procter & Gamble Company | Odorless thiols for permanent waving, straightening and depilatory applications |
| US11555021B2 (en) | 2017-07-07 | 2023-01-17 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Fatty acid derivatives and their use |
| KR20260011205A (ko) | 2017-10-05 | 2026-01-22 | 소니그룹주식회사 | 프로그램가능한 중합체성 약물 |
| CN111836645A (zh) | 2017-11-16 | 2020-10-27 | 索尼公司 | 可编程的聚合药物 |
| CN111465608A (zh) | 2017-12-13 | 2020-07-28 | 索尼公司 | 包含生物学活性化合物的离子型聚合物 |
| CN111757757A (zh) | 2017-12-21 | 2020-10-09 | 梅尔莎纳医疗公司 | 吡咯并苯并二氮呯抗体共轭物 |
| EP3737417B1 (en) | 2018-01-12 | 2025-08-27 | Sony Group Corporation | Phosphoalkyl ribose polymers comprising biologically active compounds |
| US12539334B2 (en) | 2018-01-12 | 2026-02-03 | Sony Group Corporation | Phosphoalkyl polymers comprising biologically active agents |
| CN111565756A (zh) | 2018-01-12 | 2020-08-21 | 索尼公司 | 包含生物活性化合物的具有刚性间隔基团的聚合物 |
| KR102742386B1 (ko) | 2018-03-19 | 2024-12-16 | 소니그룹주식회사 | 형광 신호 향상을 위한 2가 금속의 사용 |
| CN118480073A (zh) | 2018-03-21 | 2024-08-13 | 索尼公司 | 具有连接体基团的聚合串联染料 |
| GB201807815D0 (en) | 2018-05-14 | 2018-06-27 | Hypha Discovery Ltd | Hydroxylation techniques |
| JP7580689B2 (ja) | 2018-06-27 | 2024-11-12 | ソニーグループ株式会社 | デオキシリボースを含むリンカー基を有するポリマー色素 |
| KR20210032434A (ko) | 2018-07-13 | 2021-03-24 | 소니 주식회사 | 유기인산염 단위를 포함하는 백본을 갖는 중합체성 염료 |
| WO2020210694A1 (en) | 2019-04-11 | 2020-10-15 | Sony Corporation | Programmable polymeric drugs |
| CN113905766A (zh) | 2019-04-11 | 2022-01-07 | 索尼集团公司 | 可编程的聚合药物 |
| JP7650819B2 (ja) | 2019-04-24 | 2025-03-25 | ブイオーアール バイオファーマ インコーポレーテッド | 抗-cd45抗体薬物コンジュゲート及びその使用 |
| WO2021062176A2 (en) | 2019-09-26 | 2021-04-01 | Sony Corporation | Polymeric tandem dyes with linker groups |
| EP4038081A1 (en) | 2019-09-30 | 2022-08-10 | Sony Group Corporation | Nucleotide probes |
| US20240092820A1 (en) | 2020-11-25 | 2024-03-21 | Sony Group Corporation | Polymer dyes |
| EP4256078A1 (en) | 2020-12-07 | 2023-10-11 | Sony Group Corporation | Spacing linker group design for brightness enhancement in dimeric or polymeric dyes |
-
2018
- 2018-10-05 WO PCT/US2018/054648 patent/WO2019071153A1/en not_active Ceased
- 2018-10-05 US US16/639,499 patent/US12290571B2/en active Active
- 2018-10-05 KR KR1020207006070A patent/KR20200064059A/ko not_active Ceased
- 2018-10-05 JP JP2020508523A patent/JP7403744B2/ja active Active
- 2018-10-05 CN CN201880056126.7A patent/CN111093711A/zh active Pending
- 2018-10-05 EP EP18792814.8A patent/EP3691689A1/en active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009132020A2 (en) * | 2008-04-21 | 2009-10-29 | The Regents Of The University Of California | Selective high-affinity polydentate ligands and methods of making such |
| WO2015027176A1 (en) | 2013-08-22 | 2015-02-26 | Sony Corporation | Water soluble fluorescent or colored dyes and methods for their use |
| WO2016138461A1 (en) | 2015-02-26 | 2016-09-01 | Sony Corporation | Water soluble fluorescent or colored dyes comprising conjugating groups |
| WO2016183185A1 (en) | 2015-05-11 | 2016-11-17 | Sony Corporation | Ultra bright dimeric or polymeric dyes |
Non-Patent Citations (7)
| Title |
|---|
| "Advanced Organic Chemistry: Reactions, Mechanisms, and Structure", December 2000, WILEY |
| "Pharmaceutical Dosage Forms and Drug Delivery Systems", 1999, LIPPINCOTT WILLIAMS & WILKINS |
| "Pharmaceutical Dosage Forms", 1980, MARCEL DECKER |
| "Remington: The Science and Practice of Pharmacy", 1995, MACK PUBLISHING COMPANY |
| GREEN, T.W.; P.G.M. WUTZ: "Protective Groups in Organic Synthesis", 1999, WILEY |
| HOOVER, JOHN E.: "Remington's Pharmaceutical Sciences", 1975, MACK PUBLISHING CO. |
| JAIN NARESHKUMAR ET AL: "Current ADC Linker Chemistry", PHARMACEUTICAL RESEARCH, SPRINGER NEW YORK LLC, US, vol. 32, no. 11, 11 March 2015 (2015-03-11), pages 3526 - 3540, XP035553874, ISSN: 0724-8741, [retrieved on 20150311], DOI: 10.1007/S11095-015-1657-7 * |
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|---|---|---|---|---|
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| US11214688B2 (en) | 2018-03-30 | 2022-01-04 | Becton, Dickinson And Company | Water-soluble polymeric dyes having pendant chromophores |
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| WO2021113651A3 (en) * | 2019-12-04 | 2021-08-26 | Ashvattha Therapeutics, Inc. | Dendrimer compositions and methods for drug delivery |
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| CN115702007A (zh) * | 2020-06-01 | 2023-02-14 | Bik治疗公司 | 具有提高的药物递送和内化效率的药物偶联物 |
| JP2023534377A (ja) * | 2020-06-01 | 2023-08-09 | ビーアイケー セラピューティクス インク. | 薬物伝達と内在化効率が強化された薬物複合体 |
| AU2021284541B2 (en) * | 2020-06-01 | 2025-03-06 | Bik Therapeutics Inc. | Drug conjugate having enhanced drug delivery and internalization efficiency |
| JP7646705B2 (ja) | 2020-06-01 | 2025-03-17 | ビーアイケー セラピューティクス インク. | 薬物伝達と内在化効率が強化された薬物複合体 |
| JP2025066706A (ja) * | 2020-06-01 | 2025-04-23 | ビーアイケー セラピューティクス インク. | 薬物伝達と内在化効率が強化された薬物複合体 |
| US12180401B2 (en) | 2021-04-07 | 2024-12-31 | Becton, Dickinson And Company | Water-soluble fluorescent polymeric dyes |
Also Published As
| Publication number | Publication date |
|---|---|
| CN111093711A (zh) | 2020-05-01 |
| KR20200064059A (ko) | 2020-06-05 |
| EP3691689A1 (en) | 2020-08-12 |
| JP7403744B2 (ja) | 2023-12-25 |
| JP2020536845A (ja) | 2020-12-17 |
| US12290571B2 (en) | 2025-05-06 |
| US20200222554A1 (en) | 2020-07-16 |
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